Role of Microaneurysms in the Pathogenesis and Therapy of Diabetic Macular Edema: A Descriptive Review
Yoshihiro Takamura1, Yutaka Yamada1, Masaru Inatani1
1Department of Ophthalmology, Faculty of Medical Sciences, University of Fukui, Yoshida 910-1193, Japan.
Abstract:
Background and Objectives: This study aims to elucidate the role of microaneurysms (MAs) in the pathogenesis and treatment of diabetic retinopathy (DR) and diabetic macular edema (DME), the major causes of acquired visual impairment. Materials and Methods: We synthesized the relevance of findings on the clinical characteristics, pathogenesis, and etiology of MAs in DR and DME and their role in anti-vascular endothelial growth factor (VEGF) therapy. Results: MAs, a characteristic feature in DR and DME, can be detected by fluorescein angiography, optical coherence tomography (OCT) and OCT angiography. These instrumental analyses demonstrated a geographic and functional association between MA and ischemic areas. MA turnover, the production and loss of MA, reflects the activity of DME and DR. Several cytokines are involved in the pathogenesis of MAs, which is characterized by pericyte loss and endothelial cell proliferation in a VEGF-dependent or -independent manner. Ischemia and MAs localized in the deep retinal layers are characteristic of refractory DME cases. Even in the current anti-VEGF era, laser photocoagulation targeting MAs in the focal residual edema is still an effective therapeutic tool, but it is necessary to be creative in accurately identifying the location of MAs and performing highly precise and minimally invasive coagulation. Conclusions: MAs play a distinctive and important role in the pathogenesis of the onset, progression of DR and DME, and response to anti-VEGF treatment. Further research on MA is significant not only for understanding the pathogenesis of DME but also for improving the effectiveness of treatment.
Insights
Microaneurysms (MAs) are key in diabetic retinopathy (DR) and diabetic macular edema (DME) development and treatment response. Understanding MA dynamics improves therapies for these vision-impairing conditions.
Area of Science:
- Ophthalmology
- Diabetology
- Vascular Biology
Background:
- Diabetic retinopathy (DR) and diabetic macular edema (DME) are leading causes of vision loss.
- Microaneurysms (MAs) are central to the pathogenesis of DR and DME.
Purpose of the Study:
- To clarify the role of microaneurysms (MAs) in the pathogenesis of diabetic retinopathy (DR) and diabetic macular edema (DME).
- To investigate the significance of MAs in the context of anti-vascular endothelial growth factor (VEGF) therapy.
Main Methods:
- Synthesized findings on clinical characteristics, pathogenesis, and etiology of MAs in DR and DME.
- Reviewed the role of MAs in anti-VEGF therapy.
- Utilized fluorescein angiography, OCT, and OCT angiography for MA detection and analysis.
Main Results:
- MAs are detectable by advanced imaging and show geographic/functional links to ischemic areas.
- MA turnover correlates with DME and DR activity.
- Pathogenesis involves cytokines, pericyte loss, and VEGF-dependent/independent proliferation; deep retinal MAs indicate refractory DME.
- Laser photocoagulation targeting MAs remains effective for residual edema.
Conclusions:
- Microaneurysms are pivotal in DR and DME onset, progression, and response to anti-VEGF treatments.
- Further research into MAs is crucial for understanding DME pathogenesis and enhancing treatment efficacy.
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